The FDA did not provide a reason for the recall, but said the products had a cGMP (Current Good Manufacturing Practices) deviation.

More than 67,000 cases of roll-on deodorant that were sold nationwide have been voluntarily recalled due to an undisclosed manufacturing defect.

On July 10, Pennsylvania-based health and beauty manufacturer A.P. Deauville announced a recall of 67,214 cases of its Power Stick roll-on deodorant due to violations of Current Good Manufacturing Practice (CGMP) standards, a set of FDA-enforced guidelines designed to ensure product safety and quality.

Pennsylvania-based A.P. Deauville, LLC is recalling several types of its Power Stick deodorant, due to a process issue.

More than 67,000 cases of Power Stick deodorants were recalled for deviating from Food and Drug Administration standards.

The FDA is sounding the alarm with a deodorant recall that is impacting more than 67,000 cases of antiperspirant made by a popular manufacturer.

CHICAGO - A recall is underway for tens of thousands of cases of Power Stick antiperspirant deodorant, according to the FDA; two Chicago women allegedly stole clothes from an Oak Brook store and led police on a high-speed chase; and what started as a playful concert tradition turned into a viral PR nightmare for two tech executives.